Martin S E, Dwyer A, Kissane J M, Costa J
Cancer. 1982 Sep 1;50(5):990-6. doi: 10.1002/1097-0142(19820901)50:5<990::aid-cncr2820500529>3.0.co;2-r.
Six cases of small-cell osteosarcoma, a tumor that resembles Ewing's sarcoma but produces osteoid matrix, are presented. The patients were young (6-31 years of age) and presented with symptoms of pain and/or swelling of 1-10 months duration. The lesions demonstrated a wide variation in radiographic appearance. Histologically, the tumors were composed of small, round cells that produced variable amounts of osteoid. In three cases chondroid was also present. Two of the six patients were treated with surgery alone and four received radiation and either single- or multiple-agent adjuvant chemotherapy. The two patients who received radiation and multiple-agent adjuvant chemotherapy have no evidence of disease at four and ten years after diagnosis. Recognition of this tumor as distinct from Ewing's sarcoma and from other forms of osteosarcoma is important to determine the incidence, clinical features, and optimal therapy for this tumor.
本文报告了6例小细胞骨肉瘤病例,该肿瘤类似于尤因肉瘤,但可产生骨样基质。患者均为年轻人(年龄6 - 31岁),表现为疼痛和/或肿胀症状,持续时间为1 - 10个月。病变在影像学表现上差异很大。组织学上,肿瘤由产生不同量骨样基质的小圆形细胞组成。3例还存在软骨样成分。6例患者中有2例仅接受了手术治疗,4例接受了放疗以及单药或多药辅助化疗。接受放疗和多药辅助化疗的2例患者在诊断后4年和10年无疾病证据。认识到这种肿瘤与尤因肉瘤及其他形式的骨肉瘤不同,对于确定该肿瘤的发病率、临床特征和最佳治疗方法很重要。